An NMR Study on Diacetonefructose

  • GUO Juan ,
  • SUN Wei ,
  • GAO Xiang ,
  • SHE Meng-yao ,
  • ZONG Chun-lei
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  • 1. Key Laboratory of Synthetic and Natural Functional Molecular Chemistry, Ministry of Education, College of Chemistry & Mate rial Science, Northwest University, Xi'an 710127, China;
    2. State Key Laboratory of Continental Dynamics, Department of Geology, Northwest University, Xi'an 710029, China

Received date: 2016-05-09

  Revised date: 2017-08-02

  Online published: 2017-09-05

Abstract

2,3:4,5-bis-O-(1-methyl ethylidene)-β-D-fructopyranose is also called diacetonefructose, which is an important intermediate for drug synthesis, and contains chiral carbon atoms. In this study, one-dimensional (i.e., 1H NMR, 13C NMR and DEPT135) and two-dimensional (i.e., 1H-13C HMBC, 1H-13C HSQC, 1H-1H COSY and NOESY) NMR methods were used to elucidate the structure of this compound. The 1H and 13C NMR chemical shifts of the compound were assigned. Theoretical calculation was used to confirm the correctness of the stereochemistry configuration deduced from the NMR data.

Cite this article

GUO Juan , SUN Wei , GAO Xiang , SHE Meng-yao , ZONG Chun-lei . An NMR Study on Diacetonefructose[J]. Chinese Journal of Magnetic Resonance, 2017 , 34(3) : 329 -337 . DOI: 10.11938/cjmr20162526

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